US4707481A - Pyridazinones, their preparation and use, and bronchospasmolytic medicaments containing pyridazinones - Google Patents

Pyridazinones, their preparation and use, and bronchospasmolytic medicaments containing pyridazinones Download PDF

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US4707481A
US4707481A US06/690,655 US69065585A US4707481A US 4707481 A US4707481 A US 4707481A US 69065585 A US69065585 A US 69065585A US 4707481 A US4707481 A US 4707481A
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pyridazinone
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methoxyphenyl
methoxy
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Hermann Amschler
Wolf-Rudiger Ulrich
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Takeda GmbH
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Byk Gulden Lomberg Chemische Fabrik GmbH
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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/50—Pyridazines; Hydrogenated pyridazines
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/14—Oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
    • C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
    • C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
    • C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D237/18—Sulfur atoms

Definitions

  • the invention relates to pyridazinones, their preparation and use, and medicaments containing pyridazinones.
  • 6-Aryl-3[2H]pyridazinones as starting materials or intermediates for the synthesis of pharmaceuticals and plant protection agents and processes for their preparation are described, for example, by Baddar et al. [J.Chem. Soc. 1965, 3342], Steck [J.Heterocycl.Chem. 11(1974)755], Albright et al. [J.Heterocycl.Chem. 15(1978)881], Schreiber et al. [Bull.Soc.Chim.France 2(1973)625], Pitarch et al. [Eur.J.Med.Chem.-Chimica Therapeutica 9(1974)644] and Curran et al. [J.Med.Chem. 17(1974)273], or are known, inter alia, from the following descriptions: German Offentechnischsschrift 2,435,244, German Offenlegungsschrift 2,445,681 and German Offentechnischsschrift 2,757,923.
  • 6-Aryl-3[2H]pyridazinones with a certain action are known, for example, from the following descriptions: German Offenlegungsschrift 2,427,943, German Offenlegungsschrift 2,810,267, German Offenlegungsschrift 2,845,220, European Offenlegungsschrift 8,391, European Offenlegungsschrift 10,156, Japanese Preliminary Published Application 58,008,015 and U.S.Patent Specification 4,397,854.
  • 6-(3,4-Dimethoxyphenyl)-3[2H]pyridazinone is described by Pitarch et al. and in German Offenlegungsschrift 2,810,267.
  • the invention relates to 6-aryl-3[2H]pyridazinones of the general formula I ##STR2## wherein one of the substituents R1 or R2 denotes a methoxy group and the other denotes an alkoxy group with 2 to 5 carbon atoms or an alkenyloxy group with 3 to 5 carbon atoms and X denotes an oxygen atom or a sulfur atom, and their parmacologically acceptable salts with bases.
  • Alkoxy and alkenyloxy are straight-chain or branched. The double bond of alkenyloxy does not start from the carbon atom bonded to the oxygen atom.
  • alkoxy and alkenyloxy which may be mentioned are n-butoxy, n-propoxy, ethoxy, amyloxy, 2,2-dimethylpropyloxy, isopentyloxy, isobutoxy, sec.-butoxy, isopropoxy, buten-2-yloxy, allyloxy and methallyloxy; preferred alkoxy radicals contain 3 or 4 carbon atoms.
  • Possible salts are salts with inorganic and organic bases.
  • Cations which are used for the salt formation are, in particular, the cations of the alkali metals or alkaline earth metals, but the corresponding cations of organic nitrogen bases, such as amines or aminoalkanols, aminosugars and the like, are also used. Examples which may be mentioned are the salts of sodium, magnesium, calcium, dimethylamine, diethylamine, ethanolamine, diethanolamine, triethanolamine, glucamine, N-methylglucamine, glucosamine and N-methylglucosamine.
  • R2a denotes an alkoxy group with 2 to 4 carbon atoms or an alkenyloxy group with 3 or 4 carbon atoms and
  • Xa denotes an oxygen atom, and their pharmacologically acceptable salts with bases, form an embodiment of the invention.
  • R2b denotes a methoxy group
  • Xb denotes an oxygen atom, and their pharmacologically acceptable salts with bases, form another embodiment of the invention.
  • Preferred representatives of embodiment Ia are those in which R2a represents an n-propoxy, isopropoxy or isobutoxy group. Particularly preferred representatives are the compounds 6-(3-methoxy-4-n-propoxyphenyl)-3(2H)pyridazinone and 6-(4-isobutoxy-3-methoxyphenyl)-3(2H)pyridazinone.
  • Preferred representatives of the embodiment Ib are those in which R1b represents an n-propoxy, isopropoxy, allyl or isobutoxy group. Particularly preferred representatives are the compounds 6-(3-isobutoxy-4-methoxyphenyl)-3[2H]pyridazinone and 6-(4-methoxy-3-n-propoxyphenyl)-3[2H]pyridazinone.
  • the invention also relates to the use of the compounds according to claim 1 for the treatment or prophylaxis of diseases which are based on disorders of the bronchi and/or cardiac insufficiency, or for strengthening the heart, and to the appropriate medicaments.
  • the compounds 6-(3-methoxy-4-n-propoxyphenyl)-3[2H]pyridazinone, 6-(4-isobutoxy-3-methoxyphenyl)-3[2H]-pyridazinone and 6-(4-methoxy-3-isopropoxyphenyl)-3[2H]pyridazinone are preferred for use for the treatment or prophylaxis of diseases which are based on disorders of the bronchi, and the two first-mentioned compounds are particularly preferred.
  • the compounds 6-(3-isobutoxy-4-methoxyphenyl)-3[2]pyridazinone, 6-(4-methoxy-3-n-propoxyphenyl)-3[2H]pyridazinone and 6-(3-allyloxy-4-methoxyphenyl)-3[2H]-pyridazinone are preferred for use for the treatment or prophylaxis of diseases which are based on cardiac insufficiency, or for strengthening the heart, and the first-mentioned compound is particularly preferred.
  • the preferred medicaments are those which contain compounds whose use is preferred.
  • the oxidation (dehydrogenation) according to process variant a) is carried out by methods which are known to the expert.
  • the dehydrogenation can be carried out in the presence of noble metals of sub-group 8, for example palladium or platinum [German Offenlegungsschrift 2,757,923]; with chromium trioxide [Overend et al. J.Chem.Soc. 1947, 239] or with nitrobenzenesulfonic acids or nitronaphthalenesulfonic acids, preferably with sodium or ammonium salts thereof [British Patent Specification 1,168,291].
  • reaction according to process variant (b) is carried out by a method analogous to that of Schreiber et al. [Bull.Soc.chim.France 2(1973)625].
  • the morpholinobutyric acid III is reacted with hydrazine hydrate under reflux in a lower alkanol, for example n-butanol.
  • the morpholinium salt, of the compound III, obtained by reaction of the corresponding acetophenone with glyoxylic acid and morpholine can be reacted with hydrazine hydrate in acid solution.
  • reaction according to process variant (c) is carried out by methods which are known to the expert.
  • the compounds IV are reacted, in a manner analogous to that in German Offenlegungsschrift 2,445,681, with methanol or aqueous methanol at room temperature or slightly elevated temperature in the presence of basic compounds, such as alkali metal carbonates, hydroxides or lower alkanolates or tert.-amines, the acid is liberated from the salt formed and this acid is heated with 1 to 1.5 moles of hydrazine hydrate, at least a neutral medium, but preferably an acid medium, being maintained.
  • basic compounds such as alkali metal carbonates, hydroxides or lower alkanolates or tert.-amines
  • the arylpyridazinones I are reacted, in a manner analogous to that of Albright et al. [J.Heterocycl.Chem. 15(978)881], with phosphorus oxyhalides at 80°-120° C. in the presence of a solvent, such as toluene, xylene or chlorinated hydrocarbons, but preferably without a solvent, to give the corresponding 6-aryl-3-halogenopyridazines, reaction of which (Jahine et al.
  • the 6-aryl-3[2H]pyridazinones I are converted into the salts by methods which are known to the expert. That inorganic or organic base, the salt of which is desired, is used as the alkaline reactant.
  • the salts are obtained, for example, by reacting the pyridazinones I with the stoichiometric equivalent of the corresponding base, for example sodium hydroxide or sodium methanolate, or by converting readily soluble salts into sparingly soluble salts by double decomposition.
  • the compounds II, III and IV are known, or they can be prepared by known processes.
  • m.p. denotes melting point and the temperatures are given in °C.
  • the morpholinium salt is dissolved in 50 ml of water and the solution is acidified to pH 4.5 with acetic acid; the acid obtained as an oil is extracted with chloroform and the chloroform extract is dried over sodium sulfate and evaporated. The residue is digested with ethyl acetate, filtered off with suction and dried in vacuo. 4.9 g of the free acid of m.p. 157° are obtained.
  • Example 5 The sodium salt of 6-(3-methoxy-4-n-propoxyphenyl)-3[2H]pyridazinone
  • 6-aryl-3[2H]pyridazinones of the general formula I and those of embodiments Ia or Ib have valuable properties which render them commercially useful. Surprisingly, they are distinguished by a bronchospasmolytic and/or cardiotonic action which is in some cases considerably superior to that of theophylline or theophylline-ethylenediamine. They also have a more powerful bronchospasmolytic or positive inotropic action than 6-(4-methoxyphenyl)-3[2H]pyridazinone.
  • bronchospasmolytic activity of the 6-aryl-3[2H]pyridazinones enables them to be used in human and veterinary medicine, where they are used for the treatment and prophylaxis of diseases based on disorders of the bronchi.
  • chronic obstructive respiratory diseases of various origins bronchitis or bronchial asthma
  • the positive inotropic activity of the 6-aryl-3[2H]pyridazinones enables them to be used in human or veterinary medicine, where they are used for the treatment of diseases which are based on cardiac insufficiency or for strengthening the heart.
  • myocardial insufficiency, cardiac insufficiency, geriatric heart, myocardial infarction, cardiovascular insufficiency, angina pectoris with deficient cardiac output and coronary insufficiency are treated in humans and animals.
  • the invention thus furthermore relates to a method of treating mammals suffering from one of the abovementioned diseases.
  • the method is characterized in that a therapeutically effective and pharmacologically acceptable amount of one or more of the compounds according to the invention is administered to the diseased mammal.
  • the invention also relates to medicaments containing one or more of the 6-aryl-3[2H]pyridazinones of the general formula I or of embodiments Ia or Ib.
  • the medicaments are prepared by processes which are known per se, the compounds being used as such or, if appropriate, in combination with suitable pharmaceutical excipients. If the new pharmaceutical formulations contain pharmaceutical excipients in addition to the active compounds, the content of active compound in these mixtures is 0.5 to 95, preferably 15 to 75, per cent by weight of the total mixture.
  • the active compounds or the medicaments are used in any suitable formulation, provided that the establishment and maintenance of sufficient levels of active compound are ensured. This can be achieved, for example, by oral or parenteral administration in suitable doses.
  • the pharmaceutical formulation of the active compound is usually in the form of unit doses appropriate for the desired administration.
  • a unit dose can be, for example, a tablet, a coated tablet, a capsule, a suppository or a measured volume of a powder, of a granular material, of a solution, of an emulsion or of a suspension.
  • Unit dose in the context of the present invention is understood as a physically discrete unit which contains an individual amount of the active constituent in combination with a pharmaceutical excipient, the content of active compound in the unit dose corresponding to a fraction or multiple of a therapeutic individual dose.
  • An individual dose preferably contains the amount of active compound which is given in one administration and which usually corresponds to a whole daily dose or a half, one-third or one-quarter of the daily dose. If only a fraction, such as a half or one-quarter, of the unit dose is required for an individual therapeutic administration, the unit dose is advantageously divisible, for example in the form of a tablet with a breaking groove.
  • the pharmaceutical formulations according to the invention can contain about 5 to 250 mg, advantageously 10 to 200 mg and in particular 20 to 100 mg, of active compound.
  • Parenteral formulations can contain about 1 to 50 mg, advantageously 3 to 30 mg and in particular 5 to 25 mg, of active compound.
  • the active compound or compounds when these are given orally, are in general administered in a daily dose of 0.1 to 10 mg/kg, preferably 0.3 to 5 mg/kg and in particular 0.5 to 3 mg/kg of body weight, if appropriate in the form of several, preferably 1 to 3, individual administrations, to achieve the desired results.
  • An individual administration contains the active compound or compounds in amounts of 0.1 to 5 mg/kg, preferably 0.2 to 3 mg/kg and in particular 0.4 to 2 mg/kg of body weight.
  • Formulations for intravenous administration are expedient, in particular, for acute treatment, for example emergency treatment.
  • the therapeutic administration of the pharmaceutical formulation can take place 1 to 4 times daily at fixed or varying points in time, for example before each meal and/or in the evening. However, it may be necessary to deviate from the dosages mentioned, and in particular to do so as a function of the nature, body weight and age of the individual to be treated, the nature and severity of the disorder, the type of formulation and of administration of the medicament, and the period or interval within which administration takes place. Thus, in some cases it may be sufficient to manage with less than the abovementioned amount of active compound, whilst in other cases the abovementioned amount of active compound must be exceeded. In acute cases, a higher dose is administered at the start of the treatment. When the desired effect starts, the dose is reduced to a lower level.
  • the optimum dosage and type of administration, of the active compounds, required in each particular case can be determined by any expert on the basis of his expert knowledge.
  • the pharmaceutical formulations as a rule consist of the active compounds according to the invention and non-toxic, pharmaceutically acceptable medicament excipients, which are used as an admixture or diluent in solid, semi-solid or liquid form, or as a means of encasing, for example in the form of a capsule, a tablet coating, a sachet or some other container for the therapeutically active constituent.
  • An excipient can, for example, serve as a promoter of the absorption of the medicament by the body, as a formulating auxiliary, as a sweetener, as a flavor correctant, as a colorant or as a preservative.
  • Examples of forms which may be used orally are tablets, coated tablets, hard and soft capsules, for example made of gelatin, dispersible powders, granules, aqueous and oily suspensions, emulsions, solutions or sirups.
  • Tablets may contain inert diluents, for example calcium carbonate, calcium phosphate, sodium phosphate or lactose; granulating and dispersing agents, for example maize starch or alginates; binders, for example starch, gelatin or gum arabic; and lubricants, for example aluminum stearate or magnesium stearate, talc or silicone oil.
  • the tablets may additionally be provided with a coating, which can also be such that delayed dissolution and absorption of the medicament in the gastrointestinal tract and hence, for example, better tolerance, a protracted effect or a retarded effect are achieved.
  • Gelatin capsules can contain the medicament mixed with a solid diluent, for example calcium carbonate or kaolin, or an oily diluent, for example olive oil, groundnut oil or paraffin oil.
  • Aqueous suspensions which, if appropriate, are prepared at short notice, may contain suspending agents, for example sodium carboxymethylcellulose, methylcellulose, hydroxypropylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth or gum arabic; dispersing agents and wetting agents, for example polyoxyethylene stearate, heptadecaethyleneoxycetanol, polyoxyethylenesorbitol monooleate, polyoxyethylene sorbitan monooleate or lecithin; preservatives, for example methyl or propyl hydroxybenzoates; flavoring agents; and sweeteners, for example sucrose, lactose, sodium cyclamate, dextrose or invert sugar syrup.
  • suspending agents for example sodium carboxymethylcellulose, methylcellulose, hydroxypropylcellulose, sodium alginate, polyvinylpyrrolidone, gum tragacanth or gum arabic
  • dispersing agents and wetting agents for example polyoxyethylene stearate, h
  • Oily suspensions may contain, for example, groundnut oil, olive oil, sesame oil, coconut oil or paraffin oil, and thickeners, such as, for example, beeswax, hard paraffin or cetyl alcohol; and furthermore sweeteners, flavoring agents and antioxidants.
  • Water-dispersible powders and granules may contain the medicaments mixed with dispersing agents, wetting agents and suspending agents, for example those mentioned above, as well as with sweeteners, flavoring agents and colorants.
  • Emulsions may contain, for example, olive oil, groundnut oil or paraffin oil, in addition to emulsifying agents, such as, for example, gum arabic, gum tragacanth, phosphatides, sorbitan monooleate or polyoxyethylene sorbitan monooleate, and sweeteners and flavoring agents.
  • emulsifying agents such as, for example, gum arabic, gum tragacanth, phosphatides, sorbitan monooleate or polyoxyethylene sorbitan monooleate, and sweeteners and flavoring agents.
  • suppositories which are prepared with the aid of binders which melt at the rectal temperature, for example cacao butter or polyethylene glycol, are used.
  • sterile-injectable aqueous suspensions, isotonic salt solutions or other solutions which, if appropriate, are to be prepared at short notice and which contain dispersing agents or wetting agents and/or pharmacologically acceptable diluents, for example propylene glycol or butylene glycol, are used.
  • Oral administration of the medicaments is preferred.
  • bronchospasmolytic agent administration of the compounds according to the invention by inhalation is also preferred.
  • These compounds are administered either directly as powders or by atomizing solutions or suspensions containing the compounds according to the invention.
  • Atomizing can thereby be effected in the conventional manner, for example by compressed air atomizers or ultrasound atomizers.
  • Administration from spray cans, especially those with a conventional metering valve (metered aerosols) is particularly advantageous.
  • metered aerosols By means of metered aerosols, it is possible to provide a defined amount of active compound per spray jet.
  • So-called synchronous inhalers with which administration of the active compound can be synchronized with inhalation are of particular advantage here. Suitable synchronous inhalation devices are disclosed, for example, in German Patent Specification 1,945,257, German Patent Specification 1,917,911 and German Offenlegungsschrift 2,055,734.
  • the active compounds are preferably used in micronized form, particle sizes of less than 10 ⁇ m being advantageous.
  • the active compounds are dispersed in customary propellants, preferably with the aid of a dispersing agent.
  • propellants are, in particular, mixtures of trichlorofluoromethane (Frigen® 11) and dichlorodifluoromethane (Frigen® 12, it being possible for all or some of the trichlorofluoromethane to be replaced by 1,1,2-trichlorotrifluoroethane (Frigen® 113).
  • Possible dispersing agents are, in particular, the sorbitan esters customary for these purposes (Span® from Atlas GmbH) and lecithin.
  • the dispersing agent is dissolved in the propellant component of lower volatility, which has been initially introduced in cooled form.
  • the micronized active compound is stirred or the micronized active compounds are stirred into the solution.
  • the dispersion is filled into spray cans. After crimping, the more highly volatile propellant component is forced in.
  • the active compound or compounds can also be in micro-encapsulated form, if appropriate together with one or more of the excipients or additives mentioned.
  • 40 kg of active compound, 24 kg of lactose and 16 kg of maize starch are granulated with 4 kg of polyvinylpyrrolidone (molecular weight ⁇ 25,000) in 5.5 liters of water and the granules are forced through a sieve of 1.25 mm mesh width. After drying, 10 kg of carboxymethylcellulose, 4 kg of talc and 2 kg of magnesium stearate are added. The granules are compressed to tablets 9 mm in diameter, 250 mg in weight and with a hardness of 4 to 5 kg on a cam-type machine.
  • 150 mg of active compound, 845 mg of microcrystalline cellulose and 5 mg of amorphous silica are finely powdered, the powder is mixed thoroughly and size 4 hard gelatin capsules are filled with the mixture.
  • 6-aryl-3[2H]pyridazinones of the general formula I have a bronchospasmolytic and/or cardiotonic action which in some cases is considerably superior to that of theophylline or theophylline-ethylenediamine. In addition, they have a more powerful bronchospasmolytic or positive inotropic action than 6-(4-methoxyphenyl)-3[2H]pyridazinone, as the comparison on known experimental designs shows.
  • the relaxing action of the 6-aryl-3[2H]pyridazinones I has been tested in vitro on a chain of tracheal rings (Tr.) of guinea pigs.
  • the positive inotropic action was tested in vitro on the electrically stimulated left atrium of rats (l.a.).
  • the quotient of [EC 40pot . ] left atrium and [ED 50 ] trachea serves as a measure of the organ-selective activity.
  • the quotients of the [EC 50 ] trachea values and [ED 40pot . ] left atrium values for theophylline and the tested compound are reported as a measure of activity.
  • Isometric contractions (HSE force sensor K-30; Watanabe recorder, Linear Corder Mark 5) of isolated, left atria from rats ( ⁇ , 250-300 g) in an organ bath (10 ml, Tyrode nutrient solution, 31° C., gassing with carbogen, initial tension of the organs 0.25 g) under electrical stimulation (HSE stimulator, 7 V, 3 ms, 2 Hz) were recorded. After an equilibration time of 30 minutes, a dose-dependent increase in the contraction force can be caused by application of the test substance in cumulatively-semilogarithmically increasing concentration (for example 1 ⁇ 10 -6 +2 ⁇ 10 -6 +7 ⁇ 10 -6 +2 ⁇ 10 -5 etc.
  • the concentration of the test substance which potentiates the contraction force of the atrium by 40% compared with the starting value [EC 40pot . mol/l], expressed by the negative logarithm of the [EC 40pot mol/l]: -lg[EC 40pot ] serves as a measure of the cardiotonic activity.
  • the toxicity studies are carried out on female NMRI mice (body weight 23-30 g).
  • the animals (5 animals per dose) receive food and water ad libitum.
  • Various doses of the substances are administered once as a suspension in methocel via a gavage.
  • the period of observation lasts 7 days.
  • the tolerated dose (TD) that is to say the highest dose at which as yet none of the animals die, is determined by observation.
  • the average lethal dose (LD 50 ) that is to say the dose at which 50% of the animals die, is determined from the dose/action curve by means of linear regression.
  • Table II shows the results of testing of the inhibition of histamine-induced bronchospasm in anesthetized guinea pigs.
  • Compounds 2, 11, 15 and 16 prove to be significantly more effective than theophylline.
  • the figure in parentheses indicates the number out of 10 animals in which the latency period more than tripled.
  • the latency period is to be understood to be the time from the start of acetylcholine-atomization until clear signs of asthma appeared.
  • test procedure was derived from that of T. Olsson, Acta Allergologica 26, 438-447(1971): guinea pigs (250-350 g) in a closed plexiglass cylinder (volume 5 l) are exposed to a mist of acetylcholine (0.06% in 0.9% sodium chloride solution; Heyer Use 77 ultrasonic atomizer) twice at an interval of 20 minutes. The time from the start of atomization to the onset of clear respiratory exertion (in certain circumstances, hypoxic convulsion in the lateral position) is measured, and is denoted the latency period.
  • the latency period is 2 minutes.
  • the test substance is administered orally by gavage (standard dose 100 ⁇ mol/kg, volume 1 ml of 4% strength methocel suspension in 0.9% strength sodium chloride solution/kg).
  • gavage standard dose 100 ⁇ mol/kg, volume 1 ml of 4% strength methocel suspension in 0.9% strength sodium chloride solution/kg.
  • the animals are again exposed to the acetylcholine mist, and the latency periods are measured. Prolongation of the latency period to at least twice its length is regarded as a protective effect.
  • Table IV shows the results obtained on Langendorff guinea pig hearts with substances according to the invention compared with theophylline, amrinone and 6-(4-methoxyphenyl)-3[2H]pyridazinone (serial no. 19).
  • the compounds according to the invention show a considerably greater increasing effect on the left-ventricular pressure than do the comparison substrates. In this context, it is particularly important that the increase in the heart rate is only inconsiderable.
  • the measurement of the left-venticular pressure, the heart rate and the coronary flow was carried out on isolated and perfused hearts (Langendorff hearts) of guinea pigs ( ⁇ and ⁇ , 400-500 g). After the animals have been sacrificed by a blow to the neck and exsanguination through the carotid arteries, the thoracic cavity is opened, and the aorta is exposed and looped up with a thread. A cannula, which is attached by tubing to the apparatus from which the nutrient solution slowly drops, is introduced in the direction of the heart and the heart is, quickly after removal from the thorax, connected to the perfusion apparatus.
  • a balloon probe connected to a Statham pressure sensor, is advanced through a cut through the left atrium into the left ventricle, and is provided with an initial pressure of 40 mm Hg.
  • Coronary perfusion is carried out at constant pressure (60 cm H 2 O) from a Mariott flask containing Krebs-Henseleit solution (37° C., gassing with carbogen).
  • the nutrient solution flowing freely from the coronary sinus into the right atrium is measured with a flow meter (Grefe, Ludenscheid) and, together with the change in the left-ventricular pressure and the heart rate determined from this, is recorded on a Watanabe recorder.
  • the substances are administered in a volume of 0.1 ml of nutrient solution, in the dosage indicated in Tab. IV, within 2 sec., into the perfusion tubing close to the heart, successively in increasing doses to 5 hearts per substance and dose.
  • Table V below shows the results of measurement of the maximum rate of pressure rise in the right ventricle of guinea pigs.
  • the effect of the substances on the contractility of the heart of guinea pigs is tested on animals ( ⁇ , 400 to 1000 g) under urethane anesthesia.
  • the change in pressure in the right ventricle of the heart is measured with a tip catheter introduced through the right jugular vein and the maximum rate of pressure rise (dP/dt max ) is determined from this.
  • the heart rate is derived from the pressure waves. No noticeable increases in the heart rate were found.
  • the test substances were administered intravenously. 5-7 animals were used for each measurement, and the arithmetic mean was calculated from the results.
  • Table VI below shows the results of measurment of the percentage maximum rate of pressure rise in the left ventricles of cats.
  • the comparison compounds were amrinone and theophylline-ethylenediamine.
  • the stated dose for theophylline-ethylenediamine relates to the content of theophylline.
  • Substances 2, 5 and 7 have stronger positive inotropic effects effects (increase in dP/dtmax) than do the comparison compounds, without leading to any considerable increase in the heart rate or end-diastolic ventricular pressure.
  • the effect of the substances on the contractility of the heart in cats was tested on animals ( ⁇ , ⁇ , 3.2 to 5.2 kg) under anesthesia with chloralose/urethane.
  • the change in pressure in the left ventricle of the heart was measured with a tip catheter introduced through the right carotid artery, the R peak in the ECG (bipolar chest lead) initiating a signal to record the end-diastolic pressure; in addition, the maximum rate of pressure rise (dP/dtmax) was determined from the change in pressure.
  • the heart rate was derived from the pressure waves.
  • the test substances were administered intravenously. 2-6 animals were used per measurement, and the arithmetic mean was calculated from the results.

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US4950654A (en) * 1988-08-12 1990-08-21 Basf Aktiengesellschaft Hydrophilic theophylline powder formulation and its preparation
US5236918A (en) * 1989-04-17 1993-08-17 Byk Gulden Lomberg Chemische Fabrik Gmbh 6-aryl-3-cyanaminopyridazines, their preparation and use and medicaments containing them
US5376656A (en) * 1990-10-16 1994-12-27 Byk Gulden Lomberg Chemische Fabrik Gmbh Arylpyridazinones
US5449676A (en) * 1991-04-26 1995-09-12 Byk Gulden Lomberg Chemische Fabrik Gmbh Pyridazines
US6399611B1 (en) * 1995-04-20 2002-06-04 Merck Patent Gesellschaft Mit Beschraenkter Haftung Arylalkylpyridazinones
US6998410B2 (en) * 1997-02-17 2006-02-14 Altana Pharma Ag Compositions
US20060224190A1 (en) * 2005-04-05 2006-10-05 Jong Gill System and method for detecting heart failure and pulmonary edema based on ventricular end-diastolic pressure using an implantable medical device

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IL79280A (en) * 1985-07-05 1990-07-12 Smith Kline French Lab 4-(6-oxo-dihydro or tetrahydropyridazin-3-yl)benzene derivatives,their preparation and pharmaceutical compositions containing them
JPH06508842A (ja) * 1991-07-05 1994-10-06 ビイク　グルデン　ロンベルク　ヒエーミツシエ　フアブリーク　ゲゼルシヤフト　ミツト　ベシユレンクテル　ハフツング 置換ピリダジンの皮膚病に対する使用
ATE234270T1 (de) * 1992-12-02 2003-03-15 Pfizer Cathecoldiether als selektive pde iv hemmungsmittel
US5814651A (en) * 1992-12-02 1998-09-29 Pfizer Inc. Catechol diethers as selective PDEIV inhibitors
WO2008121877A2 (en) * 2007-04-02 2008-10-09 Institute For Oneworld Health Cftr inhibitor compounds and uses thereof

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Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4950654A (en) * 1988-08-12 1990-08-21 Basf Aktiengesellschaft Hydrophilic theophylline powder formulation and its preparation
US5236918A (en) * 1989-04-17 1993-08-17 Byk Gulden Lomberg Chemische Fabrik Gmbh 6-aryl-3-cyanaminopyridazines, their preparation and use and medicaments containing them
US5376656A (en) * 1990-10-16 1994-12-27 Byk Gulden Lomberg Chemische Fabrik Gmbh Arylpyridazinones
US5449676A (en) * 1991-04-26 1995-09-12 Byk Gulden Lomberg Chemische Fabrik Gmbh Pyridazines
US6399611B1 (en) * 1995-04-20 2002-06-04 Merck Patent Gesellschaft Mit Beschraenkter Haftung Arylalkylpyridazinones
US6998410B2 (en) * 1997-02-17 2006-02-14 Altana Pharma Ag Compositions
US20060224190A1 (en) * 2005-04-05 2006-10-05 Jong Gill System and method for detecting heart failure and pulmonary edema based on ventricular end-diastolic pressure using an implantable medical device
US7437192B2 (en) * 2005-04-05 2008-10-14 Pacesetter, Inc. System and method for detecting heart failure and pulmonary edema based on ventricular end-diastolic pressure using an implantable medical device

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AU2961784A (en) 1984-12-04
DK156655B (da) 1989-09-18
DE3462890D1 (en) 1987-05-07
IL71788A0 (en) 1984-09-30
EP0125636B1 (de) 1987-04-01
IL71788A (en) 1987-09-16
PT78566B (de) 1986-07-17
EP0125636A1 (de) 1984-11-21
ES532337A0 (es) 1985-12-01
ATE26266T1 (de) 1987-04-15
AU560607B2 (en) 1987-04-09
ZA843520B (en) 1984-12-24
DK12485D0 (da) 1985-01-10
JPS60501258A (ja) 1985-08-08
ES8601918A1 (es) 1985-12-01
WO1984004521A1 (en) 1984-11-22
DK12485A (da) 1985-01-10
NZ208107A (en) 1986-12-05
PT78566A (de) 1984-06-01
DE3417391A1 (de) 1984-11-15
DK156655C (da) 1990-02-05
CA1247100A (en) 1988-12-20
GR82072B (enrdf_load_stackoverflow) 1984-12-13

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